[Screening for deletion in patients with Duchenne's myodystrophy by multiplex amplification].
作者信息
Chukhrova A L, Malygina N A, Poliakov A V, Zaĭtseva S P, Sitnikov V F, Dadali E L, Kamennykh L N, Khrennikov V Iu, Badalian L O, Evgrafov O V
出版信息
Tsitol Genet. 1994 Jul-Aug;28(4):80-3.
PMID:7801388
Abstract
Patients with Duchenne muscular dystrophy were analyzed using the method of polymerase chain reaction in order to reveal deletions in the dystrophin gene. Deletions of different lengths and locations were detected in 28 of 78 ill boys. The highest number of deletions was detected in the 3'-end of the gene (the 45-50th exons).
摘要
Zotero 插件